drugset / Trial / NCT00117312

Extension Study Investigating the Long-Term Safety and Tolerability of Repeat Doses of FE200486 in Prostate Cancer Patients

NCT00117312

Phase 2 Terminated 37 enrolled Ferring Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

Summary

Participants responding well in Study FE200486 CS06 (NCT00117949) were given the opportunity to continue treatment with degarelix under a clinical study until FE200486 was available on the market or until the study was discontinued. Study FE200486 CS06A was to provide knowledge of the long-term safety and tolerability of FE200486.

Timeline

Start
2002-10
Primary completion
2005-11
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Degarelix Other / unclassified 40 mg Subcutaneous
Subject Degarelix Other / unclassified 80 mg Subcutaneous
Subject Degarelix Other / unclassified 120 mg Subcutaneous
Subject Degarelix Other / unclassified 160 mg Subcutaneous

Indications